| Product NDC: | 68788-6763 |
| Proprietary Name: | Promethazine VC |
| Non Proprietary Name: | Promethazinehydrochloride and phenylephrine hydrochloride |
| Active Ingredient(s): | 5; 6.25 mg/5mL; mg/5mL & nbsp; Promethazinehydrochloride and phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68788-6763 |
| Labeler Name: | Preferred Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040654 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120725 |
| Package NDC: | 68788-6763-1 |
| Package Description: | 118 mL in 1 BOTTLE (68788-6763-1) |
| NDC Code | 68788-6763-1 |
| Proprietary Name | Promethazine VC |
| Package Description | 118 mL in 1 BOTTLE (68788-6763-1) |
| Product NDC | 68788-6763 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Promethazinehydrochloride and phenylephrine hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20120725 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 5; 6.25 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |